Part:BBa_K836003:Design
lipA from B. cepacia (codon usage optimized for E. coli)
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 237
Illegal BamHI site found at 1038 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 760
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The sequence of a transcriptional terminator (biobrick BBa_B1006) was set at the end of the coding sequence. Also, to avoid RBS-CDS problems, the CDS prefix and suffix mentioned in this link (https://parts.igem.org/Assembly:RBS-CDS_issues#Standard_Assembly_and_the_RBS) were used (not in the sequence presented here).
Source
The amino sequence of this part was taken from Uniprot (lipA accesion P22088; http://www.uniprot.org/uniprot/P22088) and then codon optimization for E. coli (avoiding restriction sites for the standard assembly method) was made using the free software GeneDesigner.
References
1. Fjerbaek, L., Christensen, K. V., & Norddahl, B. (2009). A review of the current state of biodiesel production using enzymatic transesterification. Biotechnology and bioengineering, 102(5), 1298315. doi:10.1002/bit.22256
2. Ghaly, A., Dave, D., Brooks, M., & Budge, S. (2010). Production of biodiesel by enzymatic transesterification: review. American Journal of Biochemistry and Biotechnology, 6(2), 5476. Retrieved from http://www.cabdirect.org/abstracts/20103289908.html
3. Nelson, L. a., Foglia, T. a., & Marmer, W. N. (1996). Lipase-catalyzed production of biodiesel. Journal of the American Oil Chemists Society, 73(9), 11911195. doi:10.1007/BF02523383